| Description | Dexamethasoneisaglucocorticoidreceptoragonist. |
|---|---|
| IC50&Target | Glucocorticoidreceptor[1] |
| InVitro | Dexamethasoneregulatesseveraltranscriptionfactors,includingactivatorprotein-1,nuclearfactor-AT,andnuclearfactor-kB,leADIngtotheactivationandrepressionofkeygenesinvolvedintheinflammatoryresponse[1].Dexamethasonepotentlyinhibitsgranulocyte-macrophagecolonystimulatingfactor(GM-CSF)releasefromA549cellswithEC50of2.2nM.Dexamethasone(EC50=36nM)inducestranscriptionoftheβ2-receptorisfoundtocorrelatewithglucocorticoidreceptor(GR)DNAbindingandoccurredat10-100foldhigherconcentrationsthantheinhibitionofGM-CSFrelease.Dexamethasone(IC50=0.5nM)inhibitsa3×κB(NF-κB,IκBα,andI-κBβ),whichisassociatedwithinhibitionofGM-CSFrelease[2]. |
| InVivo | IthaspreviouslybeenreportedthattreatmentwithDexamethasoneatadoseof2×5mg/kgefficientlyinhibitslipopolysaccharide(LPS)-inducedinflammation.Inourexperimentalsystem,treatmentwithasingledoseofDexamethasone10mg/kg(i.p.)significantlydecreasesrecruitmentofgranulocytesaswellasspontaneousproductionofoxygenradicalscomparedwithanimalsexposetoLPSandinjectedwithsolventalone(saline).Theeffectsarestatisticallysignificantwhenadministeredboth1hbeforeand1hafterinhalationofLPS.ThenumberofgranulocytesinBALFdecreasedtolevelscomparabletohealthyanimals(givenanaerosolofwater)[3].RatstreatedwithDexamethasoneconsumelessfoodandweighedlessthancontrolrats.Treatedratsalsoweighlessthanpair-fedanimalsthoughtheirfoodintakeissimilar.FivedaysofDexamethasoneinjectionresultinasignificantincreaseinboththelivermass(+42%)andthelivertobodyweightratio(+65%).Thewetweightofgastrocnemiusmuscledecreases20%after5daysoftreatment,butitremainsunaffectedrelativetobodyweight(g/100gbodyweight),indicatingthatmuscleweightlossparalleledbodyweightloss[4]. |
| References |
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| PreparingStockSolutions |
Pleaserefertothesolubilityinformationtoselecttheappropriatesolvent. | ||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| AnimalAdministration [3][4] | Dexamethasoneispreparedinsaline(Mice)[3]. Mice[3] | ||||||||||||||||
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| MolecularWeight | 392.46 | ||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Formula | C₂₂H₂₉FO₅ | ||||||||||||
| CASNo. | 50-02-2 | ||||||||||||
| Storage |
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| Shipping | RoomtemperatureincontinentalUS;mayvaryelsewhere | ||||||||||||
| Solvent&Solubility | DMSO:≥56mg/mL Invivo:insolubleinsaline(<0.1=""> *"<1 mg/ml"="" means="" slightly="" soluble="" or="" insoluble.="" "≥"="" means="" soluble,="" but="" saturation="">1> | ||||||||||||
| References |
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Purity:98.70%
ebiomall.com
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就是蛋白质分子的小片断
是氨基酸形成的
求助各位前辈,我最近在合成的化合物水溶性很好,非常好,以至于可以随便溶解在水里,它的六氟磷酸盐也可以随意溶解在水里(大于50uM),细胞成像实验显示它根本进不去细胞,求问有没有啥方法包裹一下让它进去?我搜了一下文献,感觉多数是把脂溶性特别好的东西包裹一下弄进去的,也许是搜索姿势不对没找到我需要的答案,**点拨啊!!!
如题,之前没做过药代,老师给了一个600+Da的五肽,想测下药代动参数,看文献推荐上述两种方法,但是不知道选哪种更好,lcms前处理会不会影响小肽。
有机的是有机化合物的简称,它指的是含碳化合物.
但是,有四大类常见物质一般不作为有机物处理:
1、碳的氧化物,如CO和CO2.
2、碳酸及其盐,如CaCO3.
3、金属碳化物,如CaC2.
4、拟卤素及其化合物,如(CN)2与KSCN.
水的化学式为H2O,它不含有碳元素,故不是有机物.
但若所描述的水不是化学意义的水,而是自然界存在的天然水,那么,水中会溶有一定量的有机物.

